Phenotype #0000092602
| Individual ID |
00117368 |
| Associated disease |
STL1 |
| Phenotype details |
myopia, avascular sheets, scoliosis, cataract, retinal detachment, chorioretinal scars, optically empty vitreous |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal dominant |
| Diagnosis/Definite |
- |
| Age/Examination |
42y (42 years) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Mouna Barat-Houari |
| Database submission license |
No license selected |
| Created by |
Mouna Barat-Houari |
| Date created |
2017-08-22 17:37:19 +02:00 (CEST) |
| Date last edited |
N/A |
|